Comprehensive analysis of BRCA1, BRCA2 and TP53 germline mutation and tumor characterization: a portrait of early-onset breast cancer in Brazil.
Germline mutations in BRCA1, BRCA2 and TP53 genes have been identified as one of the most important disease-causing issues in young breast cancer patients worldwide. The specific defective biological processes that trigger germline mutation-associated and -negative tumors remain unclear. To delineat...
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2013
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oai:doaj.org-article:14eceaf0e1cf42b1a5282d76cdfa86912021-11-18T07:55:14ZComprehensive analysis of BRCA1, BRCA2 and TP53 germline mutation and tumor characterization: a portrait of early-onset breast cancer in Brazil.1932-620310.1371/journal.pone.0057581https://doaj.org/article/14eceaf0e1cf42b1a5282d76cdfa86912013-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23469205/?tool=EBIhttps://doaj.org/toc/1932-6203Germline mutations in BRCA1, BRCA2 and TP53 genes have been identified as one of the most important disease-causing issues in young breast cancer patients worldwide. The specific defective biological processes that trigger germline mutation-associated and -negative tumors remain unclear. To delineate an initial portrait of Brazilian early-onset breast cancer, we performed an investigation combining both germline and tumor analysis. Germline screening of the BRCA1, BRCA2, CHEK2 (c.1100delC) and TP53 genes was performed in 54 unrelated patients <35 y; their tumors were investigated with respect to transcriptional and genomic profiles as well as hormonal receptors and HER2 expression/amplification. Germline mutations were detected in 12 out of 54 patients (22%) [7 in BRCA1 (13%), 4 in BRCA2 (7%) and one in TP53 (2%) gene]. A cancer familial history was present in 31.4% of the unrelated patients, from them 43.7% were carriers for germline mutation (37.5% in BRCA1 and in 6.2% in the BRCA2 genes). Fifty percent of the unrelated patients with hormone receptor-negative tumors carried BRCA1 mutations, percentage increasing to 83% in cases with familial history of cancer. Over-representation of DNA damage-, cellular and cell cycle-related processes was detected in the up-regulated genes of BRCA1/2-associated tumors, whereas cell and embryo development-related processes were over-represented in the up-regulated genes of BRCA1/2-negative tumors, suggesting distinct mechanisms driving the tumorigenesis. An initial portrait of the early-onset breast cancer patients in Brazil was generated pointing out that hormone receptor-negative tumors and positive familial history are two major risk factors for detection of a BRCA1 germline mutation. Additionally, the data revealed molecular factors that potentially trigger the tumor development in young patients.Dirce Maria CarraroMaria Aparecida Azevedo Koike FolgueiraBianca Cristina Garcia LisboaEloisa Helena Ribeiro OlivieriAna Cristina Vitorino KrepischiAlex Fiorini de CarvalhoLouise Danielle de Carvalho MotaRenato David PugaMaria do Socorro MacielRodrigo Augusto Depieri MichelliEduardo Carneiro de LyraStana Helena Giorgi GrossoFernando Augusto SoaresFernando Augusto SoaresMaria Isabel Alves de Souza Waddington AchatzHelena BrentaniCarlos Alberto Moreira-FilhoMaria Mitzi BrentaniPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 8, Iss 3, p e57581 (2013) |
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Medicine R Science Q |
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Medicine R Science Q Dirce Maria Carraro Maria Aparecida Azevedo Koike Folgueira Bianca Cristina Garcia Lisboa Eloisa Helena Ribeiro Olivieri Ana Cristina Vitorino Krepischi Alex Fiorini de Carvalho Louise Danielle de Carvalho Mota Renato David Puga Maria do Socorro Maciel Rodrigo Augusto Depieri Michelli Eduardo Carneiro de Lyra Stana Helena Giorgi Grosso Fernando Augusto Soares Fernando Augusto Soares Maria Isabel Alves de Souza Waddington Achatz Helena Brentani Carlos Alberto Moreira-Filho Maria Mitzi Brentani Comprehensive analysis of BRCA1, BRCA2 and TP53 germline mutation and tumor characterization: a portrait of early-onset breast cancer in Brazil. |
| description |
Germline mutations in BRCA1, BRCA2 and TP53 genes have been identified as one of the most important disease-causing issues in young breast cancer patients worldwide. The specific defective biological processes that trigger germline mutation-associated and -negative tumors remain unclear. To delineate an initial portrait of Brazilian early-onset breast cancer, we performed an investigation combining both germline and tumor analysis. Germline screening of the BRCA1, BRCA2, CHEK2 (c.1100delC) and TP53 genes was performed in 54 unrelated patients <35 y; their tumors were investigated with respect to transcriptional and genomic profiles as well as hormonal receptors and HER2 expression/amplification. Germline mutations were detected in 12 out of 54 patients (22%) [7 in BRCA1 (13%), 4 in BRCA2 (7%) and one in TP53 (2%) gene]. A cancer familial history was present in 31.4% of the unrelated patients, from them 43.7% were carriers for germline mutation (37.5% in BRCA1 and in 6.2% in the BRCA2 genes). Fifty percent of the unrelated patients with hormone receptor-negative tumors carried BRCA1 mutations, percentage increasing to 83% in cases with familial history of cancer. Over-representation of DNA damage-, cellular and cell cycle-related processes was detected in the up-regulated genes of BRCA1/2-associated tumors, whereas cell and embryo development-related processes were over-represented in the up-regulated genes of BRCA1/2-negative tumors, suggesting distinct mechanisms driving the tumorigenesis. An initial portrait of the early-onset breast cancer patients in Brazil was generated pointing out that hormone receptor-negative tumors and positive familial history are two major risk factors for detection of a BRCA1 germline mutation. Additionally, the data revealed molecular factors that potentially trigger the tumor development in young patients. |
| format |
article |
| author |
Dirce Maria Carraro Maria Aparecida Azevedo Koike Folgueira Bianca Cristina Garcia Lisboa Eloisa Helena Ribeiro Olivieri Ana Cristina Vitorino Krepischi Alex Fiorini de Carvalho Louise Danielle de Carvalho Mota Renato David Puga Maria do Socorro Maciel Rodrigo Augusto Depieri Michelli Eduardo Carneiro de Lyra Stana Helena Giorgi Grosso Fernando Augusto Soares Fernando Augusto Soares Maria Isabel Alves de Souza Waddington Achatz Helena Brentani Carlos Alberto Moreira-Filho Maria Mitzi Brentani |
| author_facet |
Dirce Maria Carraro Maria Aparecida Azevedo Koike Folgueira Bianca Cristina Garcia Lisboa Eloisa Helena Ribeiro Olivieri Ana Cristina Vitorino Krepischi Alex Fiorini de Carvalho Louise Danielle de Carvalho Mota Renato David Puga Maria do Socorro Maciel Rodrigo Augusto Depieri Michelli Eduardo Carneiro de Lyra Stana Helena Giorgi Grosso Fernando Augusto Soares Fernando Augusto Soares Maria Isabel Alves de Souza Waddington Achatz Helena Brentani Carlos Alberto Moreira-Filho Maria Mitzi Brentani |
| author_sort |
Dirce Maria Carraro |
| title |
Comprehensive analysis of BRCA1, BRCA2 and TP53 germline mutation and tumor characterization: a portrait of early-onset breast cancer in Brazil. |
| title_short |
Comprehensive analysis of BRCA1, BRCA2 and TP53 germline mutation and tumor characterization: a portrait of early-onset breast cancer in Brazil. |
| title_full |
Comprehensive analysis of BRCA1, BRCA2 and TP53 germline mutation and tumor characterization: a portrait of early-onset breast cancer in Brazil. |
| title_fullStr |
Comprehensive analysis of BRCA1, BRCA2 and TP53 germline mutation and tumor characterization: a portrait of early-onset breast cancer in Brazil. |
| title_full_unstemmed |
Comprehensive analysis of BRCA1, BRCA2 and TP53 germline mutation and tumor characterization: a portrait of early-onset breast cancer in Brazil. |
| title_sort |
comprehensive analysis of brca1, brca2 and tp53 germline mutation and tumor characterization: a portrait of early-onset breast cancer in brazil. |
| publisher |
Public Library of Science (PLoS) |
| publishDate |
2013 |
| url |
https://doaj.org/article/14eceaf0e1cf42b1a5282d76cdfa8691 |
| work_keys_str_mv |
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